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Structure Information
Structure

Compound Identification

SMILES

CNC(=O)C1=CC=CC=C1SC1=CC2=C(C=C1)C(\C=C\C1=CC=CC=N1)=NN2[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O

InChIKey

InChIKey=YYKQABKSJYLETI-GCBNXPIGSA-N

Formula

C28H26N4O7S

Mass

562.6

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

1-pyranosylindazoles

Intermediate Tree Nodes

Not available

Direct Parent

1-pyranosylindazoles

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-pyranosylindazole - N-glucuronide - Glucuronic acid or derivatives - Glycosyl compound - N-glycosyl compound - Diarylthioether - O-sulfanylbenzoic acid or derivatives - Benzamide - Benzoic acid or derivatives - Benzopyrazole - Indazole - Aryl thioether - Benzoyl - Thiophenol ether - Beta-hydroxy acid - Monocyclic benzene moiety - Hydroxy acid - Vinylogous thioester - Benzenoid - Oxane - Pyran - Pyridine - Pyrazole - Heteroaromatic compound - Azole - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Sulfenyl compound - Thioether - Polyol - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organooxygen compound - Carbonyl group - Alcohol - Organopnictogen compound - Organonitrogen compound - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 1-pyranosylindazoles. These are nucleoside and nucleotide analogs with a structure that consists of an indazole which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.

External Descriptors

Not available

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